Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1975 1
1976 1
1979 1
1981 3
1982 1
1983 1
1984 2
1985 1
1989 1
1990 1
1991 1
1992 1
1993 1
1994 2
1995 1
1997 1
1998 1
1999 2
2000 1
2001 1
2002 1
2003 2
2004 3
2006 2
2007 1
2008 5
2009 3
2010 2
2012 1
2013 1
2014 3
2015 1
2016 5
2017 2
2018 1
2020 2
2021 4
2022 3
2023 1
2024 1

Text availability

Article attribute

Article type

Publication date

Search Results

62 results

Results by year

Filters applied: . Clear all
Page 1
Factor X deficiency.
Menegatti M, Peyvandi F. Menegatti M, et al. Semin Thromb Hemost. 2009 Jun;35(4):407-15. doi: 10.1055/s-0029-1225763. Epub 2009 Jul 13. Semin Thromb Hemost. 2009. PMID: 19598069 Review.
Diagnosis, therapeutic advances, and key recommendations for the management of factor X deficiency.
Peyvandi F, Auerswald G, Austin SK, Liesner R, Kavakli K, Álvarez Román MT, Millar CM. Peyvandi F, et al. Blood Rev. 2021 Nov;50:100833. doi: 10.1016/j.blre.2021.100833. Epub 2021 Apr 27. Blood Rev. 2021. PMID: 34024682 Free article. Review.
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. ...Consensus in treatment guidelines is still urgently needed to ensure optimal management of patients with factor X deficiency across the spectrum of
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. ...Consensus in treatment guidel
Factor X deficiency.
Uprichard J, Perry DJ. Uprichard J, et al. Blood Rev. 2002 Jun;16(2):97-110. doi: 10.1054/blre.2002.0191. Blood Rev. 2002. PMID: 12127953 Review.
The clinical phenotype is of a variable bleeding tendency. Homozygous factor X deficiency has an incidence of 1:1,000,000 in the general population. Heterozygotes are often clinically asymptomatic. Acquired factor X deficiency is rare, bu …
The clinical phenotype is of a variable bleeding tendency. Homozygous factor X deficiency has an incidence of 1:1,000,0 …
Advances in the treatment of bleeding disorders.
Peyvandi F, Garagiola I, Biguzzi E. Peyvandi F, et al. J Thromb Haemost. 2016 Nov;14(11):2095-2106. doi: 10.1111/jth.13491. Epub 2016 Oct 19. J Thromb Haemost. 2016. PMID: 27590165 Free article. Review.
Thromboembolism and bleeding in systemic amyloidosis: a review.
Nicol M, Siguret V, Vergaro G, Aimo A, Emdin M, Dillinger JG, Baudet M, Cohen-Solal A, Villesuzanne C, Harel S, Royer B, Arnulf B, Logeart D. Nicol M, et al. ESC Heart Fail. 2022 Feb;9(1):11-20. doi: 10.1002/ehf2.13701. Epub 2021 Nov 16. ESC Heart Fail. 2022. PMID: 34784656 Free PMC article. Review.
On the other hand, the bleeding risk increases because of frequent amyloid digestive involvement as well as factor X deficiency, renal failure, and increased risk of dysautonomia-related fall....
On the other hand, the bleeding risk increases because of frequent amyloid digestive involvement as well as factor X defici
62 results